Mediterranean Anemia: Diagnosis and Symptoms Explained - Family Medicine

Share to:

Mediterranean anemia


Hello Doctor, I am 36 years old and have given birth to three children.
I had surgery for an inguinal hernia at the age of 16 (at a medical center in Taipei).
I have a few questions: 1.
I was diagnosed with thalassemia in 2017, but I have had blood tests in the past that did not reveal any abnormalities.
Why was this not detected earlier? 2.
About four years ago, due to a busy work schedule, I did not have time to eat properly, and during an employee health check, I found out that my hemoglobin level was low, around 8 g/dL, but I did not have time to seek medical attention.
Could this have led to my thalassemia? 3.
I have been experiencing headaches, palpitations, and chest tightness, and despite visiting the emergency room, no blood abnormalities were found.
Can thalassemia present suddenly? I appreciate your response.
Thank you.

Yú wán tāng, 30~39 year old female. Ask Date: 2017/12/18

Dr. Liao Yaopan reply Family Medicine


Mediterranean anemia, also known as thalassemia, is a congenital blood disorder characterized by abnormal blood cells that do not appear suddenly and are not related to diet.
It is recommended to visit a hematology clinic or consult your family physician for further evaluation of the cause of anemia.
Please note: online consultations do not equate to in-person medical visits and cannot provide accurate diagnoses or treatment recommendations.
Changhua Hospital cares about your health.

Reply Date: 2017/12/18

More Info


Mediterranean anemia, also known as thalassemia, is a genetic blood disorder characterized by the body’s inability to produce adequate hemoglobin, which is essential for transporting oxygen in the blood. This condition is particularly prevalent in individuals of Mediterranean descent, but it can also affect people from other regions. Understanding the diagnosis, symptoms, and management of Mediterranean anemia is crucial for those affected by this condition.

1. Diagnosis: The diagnosis of Mediterranean anemia typically involves a combination of blood tests. These tests include a complete blood count (CBC), hemoglobin electrophoresis, and genetic testing. Hemoglobin electrophoresis is particularly important as it helps identify the different types of hemoglobin present in the blood. In your case, it is possible that previous blood tests did not include specific tests for thalassemia or that the results were not interpreted in the context of your symptoms. It is also worth noting that some individuals may have mild forms of thalassemia that do not present significant abnormalities in routine blood tests.

2. Symptoms: The symptoms of Mediterranean anemia can vary widely depending on the severity of the condition. Common symptoms include fatigue, weakness, pale skin, and shortness of breath. In more severe cases, individuals may experience more pronounced symptoms such as jaundice, dark urine, and an enlarged spleen or liver. The symptoms you mentioned, such as headaches, palpitations, and chest discomfort, can indeed be associated with anemia, particularly if your hemoglobin levels are significantly low. It is important to understand that while a busy lifestyle and inadequate nutrition can exacerbate symptoms of anemia, they do not directly cause Mediterranean anemia. This condition is inherited, and its severity can be influenced by various factors, including diet and overall health.

3. Sudden Onset: Mediterranean anemia does not typically appear suddenly; it is usually a chronic condition that develops over time. However, it is possible for individuals with mild forms of the disease to experience a sudden worsening of symptoms due to factors such as illness, stress, or nutritional deficiencies. If you have been diagnosed with thalassemia, it is essential to monitor your health closely and maintain regular check-ups with your healthcare provider. They can help manage your symptoms and provide guidance on dietary and lifestyle changes that may improve your overall well-being.

In conclusion, Mediterranean anemia is a complex condition that requires careful management and monitoring. If you have concerns about your health or the management of your anemia, it is advisable to consult with a hematologist or a healthcare provider specializing in blood disorders. They can provide personalized advice based on your medical history and current health status. Additionally, maintaining a balanced diet rich in iron and other essential nutrients can help support your overall health and mitigate some symptoms associated with anemia.

Similar Q&A

Understanding Mediterranean Anemia: Causes and Symptoms Explained

I learned about the possibility of having a condition due to a health check, so I would like to understand the causes and symptoms first.


Dr. Lin Mingxing reply Family Medicine
Mediterranean anemia, also known as thalassemia, is a congenital genetic disorder characterized by microcytic anemia, which means that the red blood cells are smaller in size and more fragile, leading to impaired function and increased susceptibility to destruction. The lifespan ...

[Read More] Understanding Mediterranean Anemia: Causes and Symptoms Explained


Understanding Mediterranean Anemia: Symptoms, Diagnosis, and Next Steps

Hello, doctor. My health check report shows the following values: white blood cell count 7030, red blood cell count 420, hemoglobin 9.3, hematocrit 32.5, mean corpuscular volume 77.4, mean corpuscular hemoglobin 22.1, mean corpuscular hemoglobin concentration 28.6, and platelet c...


Dr. Chen Yunfang reply Oncology
Hello: Common causes of anemia in young women, aside from thalassemia, include iron deficiency anemia, which is also quite prevalent. I believe your report may more likely suggest iron deficiency as the cause. You can visit a hematology clinic for a blood test to confirm. If it i...

[Read More] Understanding Mediterranean Anemia: Symptoms, Diagnosis, and Next Steps


Understanding Mediterranean Anemia: Symptoms and Testing Methods

Hello, I would like to ask about the symptoms of thalassemia and how I can check if I have it or not.


Dr. Tang Jieru reply Cardiology
Hello, Xiaoguang: Thalassemia, formerly known as Mediterranean anemia, usually has no symptoms and is often discovered incidentally during routine blood tests. A preliminary screening can be conducted through a complete blood count at the hospital, and if necessary, further serum...

[Read More] Understanding Mediterranean Anemia: Symptoms and Testing Methods


Understanding Suspected Mediterranean Anemia: Symptoms and Diagnosis

Hello Doctor: Since I was young, my father has mentioned that he was told by a physician that he might have Mediterranean anemia. My blood reports have consistently shown abnormal results. During high school, if I just woke up, I would experience a period of darkness in my vision...


Dr. Chen Yunfang reply Oncology
Hello: 1. Mediterranean anemia can only be diagnosed through hemoglobin electrophoresis (covered by health insurance) or genetic testing (out-of-pocket). The hemoglobin level, regardless of its value, cannot confirm the diagnosis; it can only raise suspicion. 2. The HBA2 level ca...

[Read More] Understanding Suspected Mediterranean Anemia: Symptoms and Diagnosis


Related FAQ

Anemia

(Family Medicine)

Anemia

(Nutrition)

Blood Test Report

(Family Medicine)

Anemia

(Oncology)

Platelets

(Family Medicine)

Hyperlipidemia

(Family Medicine)

Thalassemia

(Cardiology)

Thalassemia

(Pediatrics)

Family Medicine

(Gastroenterology and Hepatology)

Blood

(Internal Medicine)